| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g21490 | A10 | 18883954 | G | A | splice_region_variant&intron_variant | LOW | c.801+6C>T| |
S82 S92 |
| 2 | BAA10g21490 | A10 | 18885098 | C | T | missense_variant | MODERATE | c.208G>A|p.Ala70Thr |
S165 |
| 3 | BAA10g21490 | A10 | 18886528 | C | T | upstream_gene_variant | MODIFIER | c.-1102G>A| |
S124 |
| 4 | BAA10g21490 | A10 | 18887319 | G | A | upstream_gene_variant | MODIFIER | c.-1893C>T| |
S164 |
| 5 | BAA10g21490 | A10 | 18889431 | G | A | upstream_gene_variant | MODIFIER | c.-4005C>T| |
S226 |
| 6 | BAA10g21490 | A10 | 18889799 | C | T | upstream_gene_variant | MODIFIER | c.-4373G>A| |
S68 |